MULTI-SNARE SET

Catheter, Embolectomy

PFM PRODUKTE FUR DIE MEDIZIN AG

The following data is part of a premarket notification filed by Pfm Produkte Fur Die Medizin Ag with the FDA for Multi-snare Set.

Pre-market Notification Details

Device IDK011783
510k NumberK011783
Device Name:MULTI-SNARE SET
ClassificationCatheter, Embolectomy
Applicant PFM PRODUKTE FUR DIE MEDIZIN AG 15 CHEROKEE ST. Trabuco Canyon,  CA  92679
ContactSalvadore F Palomares
CorrespondentSalvadore F Palomares
PFM PRODUKTE FUR DIE MEDIZIN AG 15 CHEROKEE ST. Trabuco Canyon,  CA  92679
Product CodeDXE  
CFR Regulation Number870.5150 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2001-06-07
Decision Date2002-01-24
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
30813623011329 K011783 000
04046964349317 K011783 000
04046964349287 K011783 000
00813623011564 K011783 000
00813623011526 K011783 000
00813623011519 K011783 000
00813623011502 K011783 000
00813623011557 K011783 000
00813623011540 K011783 000
04046964349331 K011783 000
04046964349355 K011783 000
04046964349379 K011783 000
30813623011312 K011783 000
30813623011305 K011783 000
30813623011299 K011783 000
30813623011282 K011783 000
30813623011275 K011783 000
30813623011268 K011783 000
04046964349416 K011783 000
04046964349393 K011783 000
00813623011533 K011783 000

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